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Salivary Glands, Saliva and Oral Findings in COVID-19 Infection

Abstract

The world is under the threat of the novel coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Despite several efforts to contain the disease spread, it still constitutes a public health emergency of international concern. Several published reports in the scientific literature called attention of the oral cavity as the potential route of infection, the implications for dental practice and the use of saliva in the diagnose of the COVID-19. The aim of this article is to provide an overview of the literature on the salivary glands and saliva in the context of SARS-CoV-2 infection. A brief discussion of taste disturbances and oral findings in COVID-19 patients is also presented. The literature shows that SARS-CoV-2 could infect the salivary glands. It is not possible, however, to make speculations regarding them as reservoirs for the SARS-CoV-2. In addition, patients with COVID-19 presented several oral repercussions, including hyposalivation and taste disturbances. A few reports showed oral ulcers and blisters associated with SARS-CoV-2 infection. However, it remains not fully understood and might lead to erroneous assumptions. Overall, further studies are necessary to understand the real role of salivary glands and saliva in the context of SARS-CoV-2 infection.

Keywords:
Infections; Severe Acute Respiratory Syndrome; Salivary Glands; Saliva; Oral Manifestations

Keywords:
Infections; Severe Acute Respiratory Syndrome; Salivary Glands; Saliva; Oral Manifestations

Introduction

The first description of human coronavirus was published in 1965 [1[1] Tyrrell D, Bynoe M. Cultivation of a novel type of common-cold virus in organ cultures. Br Med J 1965; 1(5448):1467. https://doi.org/10.1136/bmj.1.5448.1467
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]. It has generally been thought that coronaviruses could cause future disease outbreaks [2[2] Cui J, Li F, Shi Z-L. Origin and evolution of pathogenic coronaviruses. Nat Rev Microbiol 2019; 17(3):181-92. https://doi.org/10.1038/s41579-018-0118-9
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]. Since 2002, beta coronaviruses have caused SARS-CoV in 2002-2003, MERS-CoV in 2012, and the newly emerged SARS-CoV-2 in December 2019 [3[3] Ou X, Liu Y, Lei X, Li P, Mi D, Ren L, et al. Characterization of spike glycoprotein of SARS-CoV-2 on virus entry and its immune cross-reactivity with SARS-CoV. Nat Commun 2020; 11(1):1620. https://doi.org/10.1038/s41467-020-15562-9
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]. The first case of a COVID-19, caused by SARS-CoV-2, was reported in Wuhan city, China [4[4] Zhang Y-Z, Holmes EC. A genomic perspective on the origin and emergence of SARS-CoV-2. Cell 2020; 181(2):223-7. https://doi.org/10.1016/j.cell.2020.03.035
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]. Even though has been considerable debate on the origin of the COVID-19 causative virus, reports show that it is not a purposefully manipulated virus [4[4] Zhang Y-Z, Holmes EC. A genomic perspective on the origin and emergence of SARS-CoV-2. Cell 2020; 181(2):223-7. https://doi.org/10.1016/j.cell.2020.03.035
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The SARS-CoV-2 is highly transmitted from man to man through close contact with infected patients, leading to rapid global spread by infected travelers from China [6[6] Li R, Pei S. Substantial undocumented infection facilitates the rapid dissemination of novel coronavirus (SARS-CoV-2). Science 2020; 368(6490):489-93. https://doi.org/10.1126/science.abb3221
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]. In addition, substantial undocumented infections were found to facilitate the rapid dissemination of COVID-19 [6[6] Li R, Pei S. Substantial undocumented infection facilitates the rapid dissemination of novel coronavirus (SARS-CoV-2). Science 2020; 368(6490):489-93. https://doi.org/10.1126/science.abb3221
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]. On January 30, 2020, the World Health Organization (WHO) declared that COVID-19 as a public health emergency of international concern [6[6] Li R, Pei S. Substantial undocumented infection facilitates the rapid dissemination of novel coronavirus (SARS-CoV-2). Science 2020; 368(6490):489-93. https://doi.org/10.1126/science.abb3221
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]. According to the most recent data from the Johns Hopkins Coronavirus Resource Center (https://coronavirus.jhu.edu), the global number of confirmed cases of COVID-19 was 8.407.325 with 450.716 deaths on June 18.

Several published reports had drawn attention to the oral cavity as the main route of infection [8[8] Xu H, Zhong L, Deng J, Peng J, Dan H, Zeng X, et al. High expression of ACE2 receptor of 2019-nCoV on the epithelial cells of oral mucosa. Int J Oral Sci 2020; 12(1):1-5. https://doi.org/10.1038/s41368-020-0074-x
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], the implications for dental practice [9[9] Meng L, Hua F, Bian Z. Coronavirus disease 2019 (COVID-19): emerging and future challenges for dental and oral medicine. J Dent Res 2020; 99(5):481-7. https://doi.org/10.1177/0022034520914246
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] and the potential use of saliva in the diagnose of the COVID-19 [10[10] To KK-W, Tsang OT-Y, Yip CC-Y, Chan K-H, Wu T-C, Chan JM-C, et al. Consistent detection of 2019 novel coronavirus in saliva. Clin Infect Dis 2020; ciaa149. https://doi.org/10.1093/cid/ciaa149
https://doi.org/10.1093/cid/ciaa149...
,11[11] Sabino-Silva R, Jardim ACG, Siqueira WL. Coronavirus COVID-19 impacts to dentistry and potential salivary diagnosis. Clin Oral Investig 2020; 24(4):1619-21. https://doi.org/10.1007/s00784-020-03248-x
https://doi.org/10.1007/s00784-020-03248...
]. A recent communication suggested the hyposalivation as responsible for exposing patients to a higher risk of getting coronavirus disease [12[12] Farshidfar N, Hamedani S. Hyposalivation as a potential risk for SARS‐CoV‐2 infection: inhibitory role of saliva. Oral Dis 2020; https://doi.org/10.1111/odi.13375
https://doi.org/10.1111/odi.13375...
]. Besides, taste loss was reported in COVID‐19‐positive patients [13[13] Yan CH, Faraji F, Prajapati DP, Boone CE, DeConde AS. Association of chemosensory dysfunction and Covid‐19 in patients presenting with influenza‐like symptoms. Int Forum Allergy Rh 2020; 1-8. https://doi.org/10.1002/alr.22579
https://doi.org/10.1002/alr.22579...
]. The aim of this article is to provide a brief overview of the literature on the salivary glands and saliva in the context of SARS-CoV-2 infection. A brief discussion of taste disturbances and oral findings in COVID-19 patients is also presented.

SARS-CoV-2 Infection

The SARS-CoV-2 uses angiotensin-converting enzyme-2 (ACE2) as an important receptor for entry into target cells and replication. SARS-CoV-2 employs the cellular transmembrane serine protease 2 (TMPRSS2) for spike protein priming and the inhibition of TMPRSS2 could at least partially protect against SARS-CoV-2 infection [14[14] Hoffmann M, Kleine-Weber H, Schroeder S, Krüger N, Herrler T, Erichsen S, et al. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell 2020; 181(2):271-80.e8. https://doi.org/10.1016/j.cell.2020.02.052
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]. In addition, the viral spike protein of SARS-CoV-2 appears to be dependent of sialic acid-rich proteins and monosialotetrahexosylgangliosides (gangliosides GM1) [15[15] Fantini J, Di Scala C, Chahinian H, Yahi N. Structural and molecular modeling studies reveal a new mechanism of action of chloroquine and hydroxychloroquine against SARS-CoV-2 infection. Int J Antimicrob Agents 2020; 55(5):105960. https://doi.org/10.1016/j.ijantimicag.2020.105960
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]. Gangliosides are glycosphingolipids containing sialic acid found in mammalian tissues but are most abundant in the brain [16[16] Schnaar RL. The Biology of Gangliosides. In: Baker D, Horton D. (Editor). Advances in Carbohydrate Chemistry and Biochemistry. Cambridge: Academic Press; 2019. p. 113-148.]. The gangliosides GM1 are primarily recognized as essential components of membrane rafts, which play an important role in many cellular processes, including pathogen entry [17[17] Schnaar RL, Gerardy-Schahn R, Hildebrandt H. Sialic acids in the brain: gangliosides and polysialic acid in nervous system development, stability, disease, and regeneration. Physiol Rev 2014; 94(2):461-518. https://doi.org/10.1152/physrev.00033.2013
https://doi.org/10.1152/physrev.00033.20...
].

Salivary Glands and Saliva

The three pairs of major (submandibular, parotid and sublingual) and minor salivary glands secrete saliva in the mouth. Saliva presents diverse functions, including lubrication, initiation of digestion, and immunity [18[18] Suzuki A, Iwata J. Molecular regulatory mechanism of exocytosis in the salivary glands. Int J Mol Sci 2018; 19(10):3208. https://doi.org/10.3390/ijms19103208
https://doi.org/10.3390/ijms19103208...
]. It is a biofluid rich in water, ions, and several protein groups, including mucins, which are proteins glycosylated, and most have high sialic acid content [19[19] Shogren R, Gerken TA, Jentoft N. Role of glycosylation on the conformation and chain dimensions of O-linked glycoproteins: light-scattering studies of ovine submaxillary mucin. Biochemistry 1989; 28(13):5525-36. https://doi.org/10.1021/bi00439a029
https://doi.org/10.1021/bi00439a029...
]. In addition, a range of disease biomarkers are recognized in saliva [20[20] Proctor GB. The physiology of salivary secretion. Periodontology 2000 2016; 70(1):11-25. https://doi.org/10.1111/prd.12116
https://doi.org/10.1111/prd.12116...
].

The expression of SARS-CoV-2 has been detected in the oral epithelium [8[8] Xu H, Zhong L, Deng J, Peng J, Dan H, Zeng X, et al. High expression of ACE2 receptor of 2019-nCoV on the epithelial cells of oral mucosa. Int J Oral Sci 2020; 12(1):1-5. https://doi.org/10.1038/s41368-020-0074-x
https://doi.org/10.1038/s41368-020-0074-...
] and in cough out [10[10] To KK-W, Tsang OT-Y, Yip CC-Y, Chan K-H, Wu T-C, Chan JM-C, et al. Consistent detection of 2019 novel coronavirus in saliva. Clin Infect Dis 2020; ciaa149. https://doi.org/10.1093/cid/ciaa149
https://doi.org/10.1093/cid/ciaa149...
,21[21] To KK-W, Tsang OT-Y, Leung W-S, Tam AR, Wu T-C, Lung DC, et al. Temporal profiles of viral load in posterior oropharyngeal saliva samples and serum antibody responses during infection by SARS-CoV-2: an observational cohort study. Lancet Infect Dis 2020; 20(5):565-74. https://doi.org/10.1016/S1473-3099(20)30196-1
https://doi.org/10.1016/S1473-3099(20)30...
] and swabs of human saliva [22[22] Zhang W, Du R-H, Li B, Zheng X-S, Yang X-L, Hu B, et al. Molecular and serological investigation of 2019-nCoV infected patients: implication of multiple shedding routes. Emerg Microbes Infect 2020; 9(1):386-9. https://doi.org/10.1080/22221751.2020.1729071
https://doi.org/10.1080/22221751.2020.17...
]. These studies point to the importance of saliva for diagnostic strategies. It is worth noting, however, that the source of the virus in some studies were not investigated [10[10] To KK-W, Tsang OT-Y, Yip CC-Y, Chan K-H, Wu T-C, Chan JM-C, et al. Consistent detection of 2019 novel coronavirus in saliva. Clin Infect Dis 2020; ciaa149. https://doi.org/10.1093/cid/ciaa149
https://doi.org/10.1093/cid/ciaa149...
,21[21] To KK-W, Tsang OT-Y, Leung W-S, Tam AR, Wu T-C, Lung DC, et al. Temporal profiles of viral load in posterior oropharyngeal saliva samples and serum antibody responses during infection by SARS-CoV-2: an observational cohort study. Lancet Infect Dis 2020; 20(5):565-74. https://doi.org/10.1016/S1473-3099(20)30196-1
https://doi.org/10.1016/S1473-3099(20)30...
]. In one study, the tongue of each patient was lifted and saliva was collected directly from the submandibular duct, which drains saliva from each bilateral submandibular and sublingual glands [22[22] Zhang W, Du R-H, Li B, Zheng X-S, Yang X-L, Hu B, et al. Molecular and serological investigation of 2019-nCoV infected patients: implication of multiple shedding routes. Emerg Microbes Infect 2020; 9(1):386-9. https://doi.org/10.1080/22221751.2020.1729071
https://doi.org/10.1080/22221751.2020.17...
]. Interestingly, the expression of SARS-CoV-2 was found in four out of 31 (12.90%) COVID-19 patients [23[23] Chen L, Zhao J, Peng J, Li X, Deng X, Geng Z, et al. Detection of 2019-nCoV in saliva and characterization of oral symptoms in COVID-19 patients. SSRN 2020; 2020. https://doi.org/10.2139/ssrn.3557140
https://doi.org/10.2139/ssrn.3557140...
]. Another important finding of the study of Chen and colleagues [23[23] Chen L, Zhao J, Peng J, Li X, Deng X, Geng Z, et al. Detection of 2019-nCoV in saliva and characterization of oral symptoms in COVID-19 patients. SSRN 2020; 2020. https://doi.org/10.2139/ssrn.3557140
https://doi.org/10.2139/ssrn.3557140...
] was that expression of SARS-CoV-2 was higher in critically-ill patients (3/4), which suggested the virus invasion due to high viral loads or destroyed salivary glands at the late stage of the disease [23[23] Chen L, Zhao J, Peng J, Li X, Deng X, Geng Z, et al. Detection of 2019-nCoV in saliva and characterization of oral symptoms in COVID-19 patients. SSRN 2020; 2020. https://doi.org/10.2139/ssrn.3557140
https://doi.org/10.2139/ssrn.3557140...
].

Additionally, analysis of ACE2 in human organs showed a high expression of ACE2 in minor salivary glands [24[24] Xu J, Li Y, Gan F, Du Y, Yao Y. Salivary glands: potential reservoirs for COVID-19 asymptomatic infection. J Dent Res 2020; 2020:0022034520918518. https://doi.org/10.1177/0022034520918518
https://doi.org/10.1177/0022034520918518...
]. Besides the high content of sialic acids in salivary mucin, the salivary glands were shown to present gangliosides GM1 [25[25] Nowroozi N, Kawata T, Liu P, Rice D, Zernik JH. High β-galactosidase and ganglioside GM1 levels in the human parotid gland. Arch Otolaryngol Head Neck Surg 2001; 127(11):1381-4. https://doi.org/10.1001/archotol.127.11.1381
https://doi.org/10.1001/archotol.127.11....
] and TMPRSS2 [26[26] Vaarala MH, Porvari KS, Kellokumpu S, Kyllönen AP, Vihko PT. Expression of transmembrane serine protease TMPRSS2 in mouse and human tissues. J Pathol 2001; 193(1):134-40.]. Overall, the literature suggests that SARS-CoV-2 could infect salivary glands [23[23] Chen L, Zhao J, Peng J, Li X, Deng X, Geng Z, et al. Detection of 2019-nCoV in saliva and characterization of oral symptoms in COVID-19 patients. SSRN 2020; 2020. https://doi.org/10.2139/ssrn.3557140
https://doi.org/10.2139/ssrn.3557140...
]. Given the actual body of evidence, it is not possible, however, to make speculations regarding them as reservoirs for SARS-CoV-2.

Saliva as a Diagnostic Tool

Early disease detection is crucial to reduce disease severity and prevent complications [27[27] Javaid MA, Ahmed AS, Durand R, Tran SD. Saliva as a diagnostic tool for oral and systemic diseases. J Oral Biol Craniofac Res 2016; 6(1):67-76. https://doi.org/10.1016/j.jobcr.2015.08.006.
https://doi.org/10.1016/j.jobcr.2015.08....
]. Saliva shows high potential for monitoring general health and disease due to its abundance in disease biomarkers and the advantages of being an easy, safe, cost-effective and non-invasive diagnostic approach [27[27] Javaid MA, Ahmed AS, Durand R, Tran SD. Saliva as a diagnostic tool for oral and systemic diseases. J Oral Biol Craniofac Res 2016; 6(1):67-76. https://doi.org/10.1016/j.jobcr.2015.08.006.
https://doi.org/10.1016/j.jobcr.2015.08....
,28[28] Lee Y-H, Wong DT. Saliva: an emerging biofluid for early detection of diseases. Am J Dent 2009; 22(4):241-8.]. Recent research suggests that saliva can be used as a viable diagnostic fluid for the detection of COVID-19 [11[11] Sabino-Silva R, Jardim ACG, Siqueira WL. Coronavirus COVID-19 impacts to dentistry and potential salivary diagnosis. Clin Oral Investig 2020; 24(4):1619-21. https://doi.org/10.1007/s00784-020-03248-x
https://doi.org/10.1007/s00784-020-03248...
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https://doi.org/10.7759/cureus.7708...
,30[30] Han P, Ivanovski S. Saliva - friend and foe in the COVID-19 outbreak. Diagnostics 2020; 10(5):290. https://doi.org/10.3390/diagnostics10050290
https://doi.org/10.3390/diagnostics10050...
]. Saliva was found to be even more sensitive for SARS-CoV-2 detection in COVID-19 patients than nasopharyngeal swabs [31[31] Wyllie AL, Fournier J, Casanovas-Massana A, Campbell M, Tokuyama M, Vijayakumar P, et al. Saliva is more sensitive for SARS-CoV-2 detection in COVID-19 patients than nasopharyngeal swabs. Medrxiv 2020. https://doi.org/10.1101/2020.04.16.20067835
https://doi.org/10.1101/2020.04.16.20067...
]. This biological fluid could also enable at-home self-administered sample collection for accurate large-scale SARS-CoV-2 testing [29[29] Santosh TS, Parmar R, Anand H, Srikanth K, Saritha M. A review of salivary diagnostics and its potential implication in detection of Covid-19. Cureus 2020; 12(4):e7708. https://doi.org/10.7759/cureus.7708
https://doi.org/10.7759/cureus.7708...
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https://doi.org/10.1101/2020.04.16.20067...
].

Hyposalivation

The salivary gland secretion is dependent on several factors, including temperature, circadian rhythm and intensity and type of chemosensory, masticatory, or tactile stimulation [20[20] Proctor GB. The physiology of salivary secretion. Periodontology 2000 2016; 70(1):11-25. https://doi.org/10.1111/prd.12116
https://doi.org/10.1111/prd.12116...
]. Hyposalivation, the reduction of unstimulated salivary flow rate, is a common finding in patients mainly reported as a consequence of the use of medication and psychological processes [32[32] Bergdahl M, Bergdahl J. Low unstimulated salivary flow and subjective oral dryness: association with medication, anxiety, depression, and stress. J Dent Res 2000; 79(9):1652-8. https://doi.org/10.1177/00220345000790090301
https://doi.org/10.1177/0022034500079009...
].

Dry mouth was shown to be manifested in a relatively high proportion of COVID-19 patients [23[23] Chen L, Zhao J, Peng J, Li X, Deng X, Geng Z, et al. Detection of 2019-nCoV in saliva and characterization of oral symptoms in COVID-19 patients. SSRN 2020; 2020. https://doi.org/10.2139/ssrn.3557140
https://doi.org/10.2139/ssrn.3557140...
]. A recent communication has drawn attention to hyposalivation as responsible for exposing patients to a higher risk of getting COVID-19 once the presence of many proteins with antiviral properties in saliva could be reduced [12[12] Farshidfar N, Hamedani S. Hyposalivation as a potential risk for SARS‐CoV‐2 infection: inhibitory role of saliva. Oral Dis 2020; https://doi.org/10.1111/odi.13375
https://doi.org/10.1111/odi.13375...
]. Interestingly, the SARS-CoV-2 infection is more severe in individuals over 50 years of age and with the presence of associated comorbidities such as diabetes, cardiovascular problems and diseases involving the nervous system [33[33] Fu L, Wang B, Yuan T, Chen X, Ao Y, Fitzpatrick T, et al. Clinical characteristics of coronavirus disease 2019 (COVID-19) in China: a systematic review and meta-analysis. J Infect 2020; 80(6):656-65. https://doi.org/10.1016/j.jinf.2020.03.041
https://doi.org/10.1016/j.jinf.2020.03.0...

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-35[35] Zhou F, Yu T, Du R, Fan G, Liu Y, Liu Z, et al. Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study. Lancet 2020; 395(10229):1054-62. https://doi.org/10.1016/S0140-6736(20)30566-3
https://doi.org/10.1016/S0140-6736(20)30...
]. It is known that salivary flow reduces with age and is not explained based on medications used by older adults [36[36] Affoo RH, Foley N, Garrick R, Siqueira WL, Martin RE. Meta-analysis of salivary flow rates in young and older adults. J Am Geriatr Soc 2015; 63(10):2142-51. https://doi.org/10.1111/jgs.13652
https://doi.org/10.1111/jgs.13652...
]. Besides, diabetes and medications for systemic disorders have also been associated with hyposalivation [37[37] Lopez-Pintor RM, Casanas E, Gonzalez-Serrano J. Xerostomia, hyposalivation, and salivary flow in diabetes patients. J Diabetes Res 2016; 2016:4372852. https://doi.org/10.1155/2016/4372852
https://doi.org/10.1155/2016/4372852...
,38[38] Navazesh M, Brightman VJ, Pogoda JM. Relationship of medical status, medications, and salivary flow rates in adults of different ages. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1996; 81(2):172-6. https://doi.org/10.1016/s1079-2104(96)80410-0
https://doi.org/10.1016/s1079-2104(96)80...
]. It is known that infectious and inflammatory processes might also lead to hyposalivation [39[39] Iwabuchi H, Fujibayashi T, Yamane G-y, Imai H, Nakao H. Relationship between hyposalivation and acute respiratory infection in dental outpatients. Gerontology 2012; 58(3):205-11. https://doi.org/10.1159/000333147
https://doi.org/10.1159/000333147...
,40[40] Mortazavi H, Baharvand M, Movahhedian A, Mohammadi M, Khodadoustan A. Xerostomia due to systemic disease: a review of 20 conditions and mechanisms. Ann Med Health Sci Res 2014; 4(4):503-10. https://doi.org/10.4103/2141-9248.139284
https://doi.org/10.4103/2141-9248.139284...
]. Thus, the possibility of qualitative and quantitative disturbances in saliva secretion by SARS-CoV-2 infection in the salivary gland should not be discarded.

Taste Disorders

Taste disorders have been reported in a variety of clinical problems [41[41] Doty RL. Systemic diseases and disorders. Handb Clin Neurol 2019; 164:361-87. https://doi.org/10.1016/b978-0-444-63855-7.00021-6
https://doi.org/10.1016/b978-0-444-63855...
]. Amblygeustia, a diminished sensitivity of taste, was shown to be manifested by a relatively high proportion of patients with COVID-19 [23[23] Chen L, Zhao J, Peng J, Li X, Deng X, Geng Z, et al. Detection of 2019-nCoV in saliva and characterization of oral symptoms in COVID-19 patients. SSRN 2020; 2020. https://doi.org/10.2139/ssrn.3557140
https://doi.org/10.2139/ssrn.3557140...
]. In a study, in which patients with influenza‐like symptoms underwent COVID-19 testing, smell and taste loss were reported in 68% (40/59) and 71% (42/59), respectively, of COVID‐19‐positive patients suggesting that chemosensory dysfunction should be considered when screening symptoms [13[13] Yan CH, Faraji F, Prajapati DP, Boone CE, DeConde AS. Association of chemosensory dysfunction and Covid‐19 in patients presenting with influenza‐like symptoms. Int Forum Allergy Rh 2020; 1-8. https://doi.org/10.1002/alr.22579
https://doi.org/10.1002/alr.22579...
].

Low salivary rate and disturbances in salivary biomarkers were suggested to cause xerostomia [42[42] Romero AC, Ibuki FK, Nogueira FN. Sialic acid reduction in the saliva of streptozotocin induced diabetic rats. Arch Oral Biol 2012; 57(9):1189-93. https://doi.org/10.1016/j.archoralbio.2012.02.016
https://doi.org/10.1016/j.archoralbio.20...
,43[43] Farsi NM. Signs of oral dryness in relation to salivary flow rate, pH, buffering capacity and dry mouth complaints. BMC Oral Health 2007; 7(1):15. https://doi.org/10.1186/1472-6831-7-15
https://doi.org/10.1186/1472-6831-7-15...
], which has been associated with taste sensorial complaints. Moreover, oral neuropathy or neurological transduction interruption induced by salivary compositional alterations is responsible for oral sensory complaints and loss of taste function [44[44] Hershkovich O, Nagler RM. Biochemical analysis of saliva and taste acuity evaluation in patients with burning mouth syndrome, xerostomia and/or gustatory disturbances. Arch Oral Biol 2004; 49(7):515-22. https://doi.org/10.1016/j.archoralbio.2004.01.012
https://doi.org/10.1016/j.archoralbio.20...
,45[45] Henkin RI. Decreased parotid saliva gustin/carbonic anhydrase VI secretion: an enzyme disorder manifested by gustatory and olfactory dysfunction. Am J Med Sci 1999; 318(6):380-91. https://doi.org/10.1097/00000441-199912000-00005
https://doi.org/10.1097/00000441-1999120...
]. Possible taste alterations as a result of the direct effect of SARS-CoV-2 infection in sensory neurons or other components of the peripheral gustatory system should also be considered.

Oral Findings

It is known that the oral cavity may exhibit manifestations of underlying diseases such as oral ulcerations, gingival bleeding, glossitis, oral pain, or halitosis [46[46] Gaddey HL. Oral manifestations of systemic disease. Gen Dent 2017; 65(6):23-9.]. Numerous viral diseases can affect the oral cavity, either directly or secondarily as a result of a systemic disorder. In addition, the oral manifestations of viral infections may vary but are usually manifested as either ulceration or blistering in oral tissues [47[47] Santosh ABR, Muddana K. Viral infections of oral cavity. J Family Med Prim Care 2020; 9(1):36-42. https://doi.org/10.4103/jfmpc.jfmpc_807_19
https://doi.org/10.4103/jfmpc.jfmpc_807_...

[48] Pedrosa MS, Paiva MHP, Oliveira LGFL, Pereira SMS, Silva CHV, Pompeu JGF. Oral manifestations related to dengue fever: a systematic review of the literature. Aust Dent J 2017; 62(4):404-11. https://doi.org/10.1111/adj.12516
https://doi.org/10.1111/adj.12516...
-49[49] Fourie J, Boy SC. Oral mucosal ulceration - a clinician's guide to diagnosis and treatment. S Afr Dent J 2016; 71(10):500-8.]. To the best of our knowledge, the scientific literature lacks reports of oral findings associated with previous coronaviruses. The misdiagnose of the oral findings related to COVID-19 is possible as it shares a common etiological course with several other dermatological manifestations. A case report suggested that recurrent oral ulcers could be an inaugural symptom of COVID-19 [50[50] Chaux-Bodard A-G, Deneuve S, Desoutter A. Oral manifestation of Covid-19 as an inaugural symptom? J Oral Med Oral Surg 2020; 26(2):1. https://doi.org/10.1051/mbcb/2020011
https://doi.org/10.1051/mbcb/2020011...
]. In addition, a report of three cases (two suspicious and one confirmed) showed that pain and intraoral manifestations such as oral ulcers or blisters before seeking medical advice were a common finding in COVID-19 [51[51] Martín Carreras‐Presas C, Amaro Sánchez J, López‐Sánchez AF, Jané‐Salas E, Somacarrera Pérez ML. Oral vesiculobullous lesions associated with SARS‐CoV‐2 infection. Oral Dis 2020. https://doi.org/10.1111/odi.13382
https://doi.org/10.1111/odi.13382...
]. Thus, it was encouraged to perform intraoral examinations in patients suspected of SARS-CoV-2 [51[51] Martín Carreras‐Presas C, Amaro Sánchez J, López‐Sánchez AF, Jané‐Salas E, Somacarrera Pérez ML. Oral vesiculobullous lesions associated with SARS‐CoV‐2 infection. Oral Dis 2020. https://doi.org/10.1111/odi.13382
https://doi.org/10.1111/odi.13382...
].

As the oral findings are still new in the literature, their occurrence may vary significantly among COVID-19 patients and, thus, the associated systemic diseases and/or poor oral health may be a contributory factor to the oral presentations. Given the possibility of immunocompromised statuses of the patients, it is also possible that the oral manifestations may be related to other viruses (e.g., herpes simplex, varicella zoster, and human immunodeficiency) [47[47] Santosh ABR, Muddana K. Viral infections of oral cavity. J Family Med Prim Care 2020; 9(1):36-42. https://doi.org/10.4103/jfmpc.jfmpc_807_19
https://doi.org/10.4103/jfmpc.jfmpc_807_...

[48] Pedrosa MS, Paiva MHP, Oliveira LGFL, Pereira SMS, Silva CHV, Pompeu JGF. Oral manifestations related to dengue fever: a systematic review of the literature. Aust Dent J 2017; 62(4):404-11. https://doi.org/10.1111/adj.12516
https://doi.org/10.1111/adj.12516...
-49[49] Fourie J, Boy SC. Oral mucosal ulceration - a clinician's guide to diagnosis and treatment. S Afr Dent J 2016; 71(10):500-8.]. As research is still ongoing and intraoral examinations have not yet been considered when screening for this disease, literature still lacks evidence to understand better the underlying mechanisms of the oral findings in COVID-19 patients. Thus, it is not possible to affirm that the oral findings, reported in the literature, are direct manifestations of SARS-CoV-2 infection.

Conclusion

The SARS-CoV-2 infection is responsible for several events in the mouth, including hyposalivation and taste disturbances. A few reports showed oral ulcers and blisters associated with SARS-CoV-2 infection. However, it remains not fully understood and might lead to erroneous assumptions. Studies are necessary to understand the real role of salivary glands and saliva in this disease context.

  • Financial Support
    This study was supported by the São Paulo Research Foundation (Grant No. 2019/14556-7) and the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001.

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Edited by

Academic Editor: Yuri Wanderley Cavalcanti

Publication Dates

  • Publication in this collection
    29 July 2020
  • Date of issue
    2020

History

  • Received
    25 May 2020
  • Accepted
    03 June 2020
  • Published
    19 June 2020
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